United Kingdom MHRA device registration 205854

Inspiratory line humidification chamber, single-use

United Kingdom·General Medical Device·Fisher & Paykel Healthcare Ltd·Registered Nov 27, 2024DREGIY

Registration details

Device ID: 205854
Status: DREGIY
Date Registered: Nov 27, 2024

Device classification

Device Type: General Medical Device
Type: Class IIa

Manufacturer

Name: Fisher & Paykel Healthcare Ltd
Address: 15 Maurice Paykel Place, East Tamaki
Auckland, Auckland, New Zealand

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About this record

Inspiratory line humidification chamber, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 205854. The device is manufactured by Fisher & Paykel Healthcare Ltd from New Zealand, classified as General Medical Device.

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